chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18916285489162855AG17GENIChomozygous942828106
18916353489163535TC19GENIChomozygous942828107
18916399789163998GA41GENIChomozygous942828108
18916457589164576GA18GENIChomozygous942828109
18916460189164602TC22GENIChomozygous942828110
18916471989164720TC27GENIChomozygous942828111
18916476089164761CA28GENIChomozygous942828112
18916530789165308TC24GENIChomozygous942828113
18916634589166346CT17GENIChomozygous942828114
18916721689167217AT22GENIChomozygous942828115
18916760989167610CT33GENIChomozygous942828116
18916824489168245GA26GENIChomozygous942828117
18916825489168255TC23GENIChomozygous942828118
18916827789168278CT28GENIChomozygous942828119
18916833889168339AG33GENIChomozygous942828120
18916838089168381AG32GENIChomozygous942828121
18916842589168426GT26GENIChomozygous942828122
18916899889168999AG23GENIChomozygous942828123
18916920589169206AC34GENIChomozygous942828124
18916981889169819CT29GENIChomozygous942828125
18917020589170206AG21GENIChomozygous942828126
18917090289170903AG21GENIChomozygous942828127
18917178289171783CT32GENIChomozygous942828128
18917239189172392GA25GENIChomozygous942828129
18917313189173132CT33GENIChomozygous942828130
18917324089173241TA48GENIChomozygous942828131
18917379689173797AG28GENIChomozygous942828132
18917439089174391TC28GENIChomozygous942828133
18917451989174520TC25GENIChomozygous942828134
18917542289175423AT33GENIChomozygous942828135